Technical Writer

KEY RESPONSIBILITIES
· Work with R&D, regulation and QA teams to obtain an in-depth understanding of the platform and the documentation requirements
· Create and maintain release notes
· Create and maintain user manuals
· Full documentation lifecycle – create, standardize across the company, maintain continuity and consistency of style of content, revise as new issues arise
REQUIREMENTS
· 5+ years of experience in Technical Writing for Medical Device company
· Engineering degree (Mechanical or Electrical) – big advantage
· Experience with documentation per FDA/CE design control and ISO 13485
· Understanding of engineering best practices and test methodologies
· Manage multiple tasks and priorities simultaneously and adapt to changes in program priorities
· Excellent communication and interpersonal skills
· Excellent English language skills